Liquid crystal composition and liquid crystal display device containing the same

Abstract

The present invention provides a liquid crystal composition and a liquid crystal display device containing the same, wherein the liquid crystal composition comprises at least two compounds of general formula B, at least one compound of general formula I, at least one polymerizable compound of general formula RM and at least one self-aligning agent of general formula SA. The liquid crystal composition of the present invention has a higher clearing point, optical anisotropy, a larger absolute value of dielectric anisotropy, a K value, a smaller rotational viscosity, a lower residue concentration, a faster angular velocity, a smaller surface roughness of the polymer layer, and a longer low-temperature storage time, so that the liquid crystal display device has a wider temperature use range, a smaller threshold voltage, a better contrast, a faster response speed, and can achieve vertical alignment of liquid crystal molecules without a PI alignment layer, and can accelerate the production process of PSA-type liquid crystal displays, and effectively improve the problems of "image viscosity", uneven display, and "broken bright spots" existing in existing PSA-type liquid crystal displays. #imgabs0#

Description

Technical Field

[0001] The present invention relates to the field of liquid crystals, in particular to a liquid crystal composition and a liquid crystal display device comprising the liquid crystal composition. Background Art

[0002] Liquid crystal display (LCD) has achieved rapid development due to its small size, light weight, low power consumption and excellent display quality, and has been widely used in portable electronic information products. According to the type of display mode, LCD can be divided into PC (phase change), TN (twist nematic), STN (super twisted nematic), ECB (electrically controlled birefringence), OCB (optically compensated bend), IPS (in-plane switching), FFS (fringe field switching), VA (vertical alignment) and PSA (polymer stable alignment).

[0003] The liquid crystal display element contains a nematic liquid crystal composition, and the liquid crystal composition has appropriate characteristics. By improving the characteristics of the liquid crystal composition, an AM element with good characteristics can be obtained. The relationship between the characteristics of the liquid crystal composition and the AM element is summarized in the following Table A. The characteristics of the liquid crystal composition are further described based on commercially available AM ​​elements. The temperature range of the nematic phase is related to the temperature range of the element. The viscosity of the liquid crystal composition is related to the response time of the element. In order to make the element display dynamic images, it is preferred that the response time of the element is short.

[0004] Table A Characteristics of liquid crystal composition and AM element

[0005] serial number Characteristics of Liquid Crystal Compositions Characteristics of AM components 1 Nematic phase has a wide temperature range Wide temperature range 2 Low viscosity Short response time 3 Large optical anisotropy High contrast 4 The absolute value of dielectric anisotropy is large Low threshold voltage, low power consumption, high contrast 5 Larger specific resistance High voltage holding rate and contrast 6 UV and heat stable Long life 7 Large elastic constant High contrast, short response time, fast response speed

[0006] In the application of liquid crystal display devices, the contrast has a critical impact on visual effects. Generally speaking, the greater the contrast, the clearer and more eye-catching the image, and the brighter the color; on the contrary, if the contrast is small, the whole picture will be gray. High contrast is of great help to the clarity, detail and grayscale performance of the image. High-contrast products have advantages in black and white contrast, clarity, integrity and other aspects. Contrast also has a great impact on the display effect of dynamic video. Since the light and dark conversion in dynamic images is relatively fast, the higher the contrast, the easier it is for the human eye to distinguish such a conversion process.

[0007] In order to improve the response speed of liquid crystal display devices, it is necessary to reduce the rotational viscosity of liquid crystal materials as much as possible. However, generally, low-viscosity liquid crystal materials have lower clearing points and optical anisotropy, so when formulating liquid crystal compositions, it is necessary to consider other performance requirements while reducing the viscosity.

[0008] The PSA type liquid crystal display mode is to add a small amount (for example, 0.3wt%, more typically <1wt%) of one or more polymerizable compounds to the liquid crystal composition, which can ensure that after the liquid crystal composition is filled into the liquid crystal box, the liquid crystal molecules are polymerized or cross-linked in situ (usually by UV light polymerization) in a state with an initial orientation when a voltage is applied between the electrodes or when no voltage is applied, thereby fixing the orientation of the liquid crystal molecules. With the continuous development of PSA type liquid crystal display elements, they are applied to various traditional liquid crystal display devices, such as the known PSA-VA, PSA-OCB, PSA-IPS, PSA-FFS and PSA-TN type liquid crystal displays. In a PSA type liquid crystal display, a liquid crystal composition containing a polymerizable compound is located between two substrates, each substrate is equipped with an electrode structure, or two electrode structures are placed on only one of the substrates. In addition, either or both of the two substrates may contain an alignment layer disposed on the substrate or the electrode structure (if present) to induce the initial alignment of the liquid crystal composition. Like conventional liquid crystal displays, PSA type liquid crystal displays can be operated as active matrix or passive matrix displays. In the case of active-matrix displays, the individual pixels are addressed by means of integrated non-linear active elements, such as transistors; in the case of passive-matrix displays, the individual pixels are usually addressed according to multiplexing methods known in the art.

[0009] After the liquid crystal composition is filled into the display device, the polymerizable compounds contained in the liquid crystal composition are usually polymerized or crosslinked in situ by UV photopolymerization, wherein the UV photopolymerization is achieved by exposing the liquid crystal composition to UV radiation, and preferably a voltage is applied to the electrode structure at the same time. As a result of UV exposure, the polymerized or crosslinked polymerizable compounds are phase separated from other compounds in the liquid crystal composition and form a polymer layer on the surface of the substrate, where they cause a pre-tilt angle of the liquid crystal molecules relative to the substrate. For PSA-VA, PSA-OCB, PSA-FFS and PSA-TN type liquid crystal displays, the polymerization of the polymerizable compounds is preferably carried out under the application of voltage; for PSA-IPS displays, it is possible to apply or not apply a voltage, preferably without applying a voltage.

[0010] Generally, in the production method of PSA type liquid crystal display, UV photopolymerization is achieved through the following two steps:

[0011] In the first step (hereinafter referred to as the "UV1 step"), the liquid crystal composition is exposed to UV radiation emitted by a radiation source (hereinafter referred to as the "light source"), and a voltage is applied to the electrode structure, thereby generating a pre-tilt angle. The more preferred polymerizable compound should generate a smaller pre-tilt angle at the same time or generate the same pre-tilt angle at a shorter UV1 radiation time (i.e., a faster angular velocity) to improve production efficiency, shorten the tact time during mass production, and reduce costs; at the same time, the faster the angular velocity of the polymerizable compound, the more conducive it is to achieve complete polymerization of the polymerizable compound, thereby reducing polymer residues. In order to increase the angular velocity, it is preferred to use UV1 radiation with a shorter wavelength; and in order to increase the voltage holding ratio (Voltage Holding Ratio, VHR), it is preferred to use UV1 radiation with a longer wavelength. Therefore, it is usually difficult to take both faster angular velocity and higher voltage holding ratio into account.

[0012] In the second step (hereinafter referred to as "UV2 step"), the liquid crystal composition is exposed to UV irradiation conditions without applying voltage to the electrode structure to ensure that the residual polymerizable compound that has not been polymerized in the UV1 step can be completely polymerized. It is expected that after the UV2 step, the change in the pre-tilt angle is as small as possible to reduce the possibility of uneven display of the PSA type liquid crystal display due to the unevenness of the UV process (uneven external conditions such as light, heat, stress, etc.). At the same time, the UV radiation intensity in the UV2 step should be reduced to avoid or reduce negative effects (such as reduced reliability or image stickiness).

[0013] With the application of PSA liquid crystal display technology, people have found that not all liquid crystal compositions can be perfectly matched with polymerizable compounds. After UV1 and UV2 treatment, there may be problems such as residual polymerizable compounds failing to polymerize completely and slow pre-tilt angle formation speed. At the same time, the poor mutual solubility of liquid crystal compositions and polymerizable compounds will make the polymer network formed after the polymerization of polymerizable compounds poor in rigidity, resulting in changes in the structure of the polymer network when the PSA liquid crystal display element continuously displays the same pattern for a long time, which in turn causes changes in the pre-tilt angle of the liquid crystal molecules, resulting in poor display.

[0014] In the current production of PSA-type liquid crystal displays, it is necessary to coat a layer of polyimide (PI) alignment layer (PI alignment layer for short) on the glass substrate to achieve vertical alignment of liquid crystal molecules, but this method has obvious shortcomings (such as the PI coating process is cumbersome, complicated, and time-consuming), and there are many other adverse effects, which greatly limit the quality of liquid crystal displays. The PI alignment process greatly reduces production efficiency and increases production costs; at the same time, due to the limited ability to accurately control the PI printing area, and the deviation of the PI printing area will affect the sealant sealing of narrow-frame products and the display effect of the edge, it greatly limits the development of current mainstream narrow-frame products and greatly reduces the yield rate of its production. In the prior art, the use of the PI alignment layer is mainly replaced by adding a self-aligning agent to the liquid crystal composition, but not all liquid crystal compositions can be perfectly matched with polymerizable compounds and self-aligning agents. After the UV1 step and the UV2 step, there may be problems such as residues of polymerizable compounds and self-aligning agents, slow angular velocity of the pre-tilt angle, and uneven surface of the polymer layer. At the same time, the poor miscibility of the liquid crystal composition and the polymerizable compound will result in poor rigidity of the polymer network formed after the polymerization of the polymerizable compound, which will cause the structure of the polymer network to change when the PSA-type liquid crystal display element displays the same pattern continuously for a long time, and then cause the pre-tilt angle of the liquid crystal molecules to change, resulting in poor display.

[0015] In addition, the liquid crystal compound still has some disadvantages in its application in a PSA type liquid crystal display after being mixed with a polymerizable compound and a self-aligning agent. It is required that the liquid crystal compound and the selected polymerizable compound and the liquid crystal composition formed by the combination of the self-aligning agent have a lower rotational viscosity and good photoelectric properties to achieve the expected display effect. The length of the polymerization process of the polymerizable compound directly affects the time required for the preparation process of the liquid crystal display element or the liquid crystal display device, but under normal circumstances, if the polymerization speed is too fast, it is easy to form large particle polymers, which is easy to cause the occurrence of poor display such as "broken bright spots". Due to the uneven size of the polymer particles, the distribution of the polymer is also uneven, which in turn causes the problem of uneven display. Therefore, the problem that still needs to be solved is: to make the liquid crystal composition have a faster polymerization speed, uniform polymer particles (that is, a smaller surface roughness of the polymer layer), and improved poor display problems such as "image viscosity", uneven display, and "broken bright spots".

[0016] In addition, with the development of display technology, the liquid crystal display industry has stricter requirements on the display quality of LCDs, especially in the TV industry. As TV sizes generally increase, LCD generation lines also increase, and the difficulty of manufacturing large-size LCD panels also increases significantly. Therefore, how to ensure display quality is an urgent problem to be solved. At the same time, in addition to continuously optimizing the panel manufacturing process, the development of liquid crystal materials is also one of the solutions. Especially for PSA-type liquid crystal displays, the selection of liquid crystal compositions used in combination with polymerizable compounds has become a research hotspot.

[0017] Therefore, the research focus in this field is to develop liquid crystal materials with fast polymerization speed, controllable polymerization process and good comprehensive performance to meet the needs of PSA type liquid crystal display elements, and to provide display technology that can achieve vertical alignment of liquid crystal molecules without the need for a PI alignment layer. Summary of the invention

[0018] Purpose of the invention: In view of the defects of the prior art, the purpose of the present invention is to provide a liquid crystal composition, which has a small polymer residue, good pre-tilt angle stability, and a small polymer layer surface roughness while maintaining an appropriate clearing point, an appropriate optical anisotropy, an appropriate absolute value of dielectric anisotropy, a large K value and a small rotational viscosity, so that a liquid crystal display device containing the liquid crystal composition has a good contrast, a fast response speed, and can achieve vertical alignment of liquid crystal molecules without a PI alignment layer while maintaining a wide temperature use range and a small threshold voltage, and can effectively accelerate the production process of PSA-type liquid crystal displays and improve production efficiency. At the same time, it can effectively improve the problems of "image viscosity", uneven display, and "broken bright spots" existing in existing PSA-type liquid crystal displays, and has a high practical application value.

[0019] Another object of the present invention is to provide a liquid crystal display device comprising the liquid crystal composition.

[0020] Technical solution: In order to achieve the above invention objectives, the present invention provides a liquid crystal composition, the liquid crystal composition comprising:

[0021] At least two compounds of formula B

[0022]

[0023] At least one compound of formula I

[0024]

[0025] At least one polymerizable compound of the general formula RM

[0026] as well as

[0027] At least one self-aligning agent of the general formula SA

[0028]

[0029] in,

[0030] R B1 and R B2 Each independently represents halogen, -CF3, -OCF3, a linear or branched alkyl group containing 1 to 12 (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12) carbon atoms, The straight or branched alkyl group containing 1 to 12 carbon atoms, One or more non-adjacent -CH2- in the above mentioned group may be independently replaced by -O-, -S-, -CH=CH-, -C≡C-, -CO-, -CO-O- or -O-CO-, and one or more -H in the straight or branched alkyl group containing 1 to 12 carbon atoms may be independently replaced by -F or -Cl;

[0031] R 11 and R 12 Each independently represents a straight-chain or branched alkyl group containing 1-12 (for example, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11) carbon atoms, and one or more non-adjacent -CH2- in the straight-chain or branched alkyl group containing 1-12 carbon atoms can be independently replaced by -C=C-, -C≡C-, -O-, -CO-, -CO-O- or -O-CO-;

[0032] R1 represents -H, halogen, -CN, -Sp2-P2, a straight or branched chain alkyl group containing 1 to 12 carbon atoms (e.g., 2, 3, 4, 5, 6, 7, 8, 9, 10, 11), wherein the straight or branched alkyl group containing 1 to 12 carbon atoms, One or more non-adjacent -CH2- may be independently replaced by -CH=CH-, -C≡C-, -O-, -CO-, -CO-O- or -O-CO-, and one or more -H may be independently replaced by -F or -Cl;

[0033] R S1 Indicates -Sp 1 -P 1 , a straight or branched alkyl group containing 1 to 12 (e.g., 2, 3, 4, 5, 6, 7, 8, 9, 10, or 11) carbon atoms, wherein one or more non-adjacent -CH2- in a straight-chain or branched alkyl group containing 1 to 12 carbon atoms can be independently replaced by -CH=CH-, -C≡C-, -O-, -CO-, -CO-O- or -O-CO-, and wherein a straight-chain or branched alkyl group containing 1 to 12 carbon atoms, One or more -H in can be independently replaced by -F or -Cl;

[0034] ring and ring Each independently expresses in One or more -CH2- in the ring may be replaced by -O-, and one or more single bonds in the ring may be replaced by double bonds, wherein One or more -H in the ring may be independently replaced by -CN, -F or -Cl, and one or more -CH= in the ring may be replaced by -N=;

[0035] ring and ring Each independently expresses in One or more -CH2- in the ring may be replaced by -O-, and one or more single bonds in the ring may be replaced by double bonds, wherein One or more -H in the group may be replaced independently by -F, -Cl, -CN, -Sp3-P3, a halogenated or unhalogenated straight-chain alkyl group containing 1 to 12 carbon atoms, a halogenated or unhalogenated straight-chain alkoxy group containing 1 to 11 carbon atoms, substituted, and -CH= in one or more rings may be replaced by -N=;

[0036] ring express in One or more -H in the group may be replaced independently by -F, -Cl, -CN, -Sp3-P3, a halogenated or unhalogenated straight-chain alkyl group containing 1 to 12 carbon atoms, a halogenated or unhalogenated straight-chain alkoxy group containing 1 to 11 carbon atoms, substituted, and -CH= in one or more rings may be replaced by -N=;

[0037] ring express in One or more -CH2- in the ring may be replaced by -O-, and one or more single bonds in the ring may be replaced by double bonds;

[0038] Ls1 and Ls3 each independently represent -F, -Cl, -CN, -NO2, -NCO, -NCS, -OCN, -SCN, -C(O)N(R S0 )2. -C(O)R S0 , a straight or branched alkyl group containing 1 to 12 (e.g., 2, 3, 4, 5, 6, 7, 8, 9, 10, or 11) carbon atoms, wherein one or more non-adjacent -CH2- in a straight-chain or branched alkyl group containing 1 to 12 carbon atoms can be independently replaced by -CH=CH-, -C≡C-, -O-, -CO-, -CO-O- or -O-CO-, and wherein a straight-chain or branched alkyl group containing 1 to 12 carbon atoms, One or more -H in the above-mentioned may be independently replaced by -F, wherein R S0 represents a straight or branched alkyl group containing 1 to 12 (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12) carbon atoms;

[0039] Ls2 stands for -Sp 3 -P 2 or

[0040] R S2 and R S3 Each independently represents an anchoring group, the anchoring group is Where * indicates the connection site in the bonded structure;

[0041] p represents 1 or 2, wherein when p represents 2, -Sp 8 -X 2Can be the same or different;

[0042] o means 0 or 1;

[0043] M S1 express

[0044] I S1 and J S1 Each independently represents -CH2-, -O- or -S-;

[0045] N S1 Indicates =O or =S;

[0046] V K1 、V K2 and V K3 Each independently represents -CH= or -N=;

[0047] X 1 and X 2 Each independently represents -H, -OH, -SH, -NH2, -NHR 11 、-N(R 11 )2. -NHC(O)R 11 、-OR 11 , -C(O)OH, -CHO, or a linear or branched halogenated or unhalogenated alkyl group containing 1 to 12 (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12) carbon atoms, wherein X 1 and X 2 At least one of -OH, -SH, -NH2, -NHR 11 , -C(O)OH and -CHO, where R 11 represents a straight or branched alkyl group containing 1 to 12 (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12) carbon atoms;

[0048] P1, P2, P3, P 1 , P 2 and P 3 each independently represents a polymerizable group;

[0049] Sp1, Sp2, Sp3, Sp 1 、Sp 2 、Sp 3 、Sp 4 、Sp 5 、Sp 7 and Sp 8 each independently represents a spacer group or a single bond;

[0050] Sp 6 Each independently expresses

[0051] Z1, Z2, Z 1 and Z 2 Each independently represents -O-, -S-, -CO-, -CO-O-, -O-CO-, -O-CO-O-, -CH2O-, -OCH2-, -CH2S-, -SCH2-, -CF2O-, -OCF2-, -CF2S-, -SCF2-, -(CH2) d -, -CF2CH2-, -CH2CF2-, -(CF2) d -, -CH=CH-, -CF=CF-, -CH=CF-, -CF=CH-, -C≡C-, -CH=CH-CO-O-, -O-CO-CH=CH-, -CH2CH2-CO-O-, -O-CO-CH2CH2-, -CHR 1 -、-CR 1 R 2 - or a single bond, where R 1 and R 2 Each independently represents a straight or branched alkyl group containing 1 to 12 carbon atoms, and d represents an integer of 1 to 4;

[0052] X B and X0 each independently represent -O-, -S- or -CO-;

[0053] L B1 and L B2 Each independently represents -H, -F, -Cl, -CF3 or -OCF3;

[0054] Z B1 and Z B2 Each independently represents a single bond, -O-, -S-, -CO-O-, -O-CO-, -CH2O-, -OCH2-, -CH=CH-, -C≡C-, -CH2CH2-, -CF2CF2-, -(CH2)4-, -CF2O- or -OCF2-;

[0055] n B1 and n B2 Each independently represents 0, 1 or 2. B1 When it indicates 2, the ring can be the same or different, where n B2 When it indicates 2, the ring Can be the same or different, Z B2 Can be the same or different;

[0056] n 11 Indicates 1 or 2;

[0057] ns1 Indicates 1, 2, or 3, n s2 represents 1, 2, 3, or 4, and n s1 +n s2 ≥3, where n s1 When it means 2 or 3, can be the same or different, where n s2 When it means 2, 3 or 4, Can be the same or different;

[0058] p s1 、p s2 、p s3 and p s4 Each independently represents 0, 1 or 2, where p s1 When p represents 2, Ls2 can be the same or different. s2 When p represents 2, Ls1 can be the same or different. s3 When it means 2, -Sp 5 -R S3 can be the same or different, where p s4 When 2 is represented, Ls3 may be the same or different; and

[0059] a represents 0, 1 or 2, b represents 0 or 1, wherein when a represents 2, the ring can be the same or different, and Z1 can be the same or different.

[0060] In some embodiments of the present invention, the compound of formula B is selected from the group consisting of the following compounds:

[0061]

[0062] as well as

[0063] in,

[0064] R B1 ' and R B2 ' Each independently represents a straight or branched alkyl group containing 1 to 12 carbon atoms.

[0065] In the present invention, in order to obtain a higher clearing point, appropriate optical anisotropy, a larger absolute value of dielectric anisotropy, a larger K value, a lower residue concentration, a faster angular velocity, a smaller surface roughness of the polymer layer and a longer low-temperature storage time, the liquid crystal composition preferably contains at least two compounds of general formula B.

[0066] In some embodiments of the present invention, it is preferred to adjust the content of the compound of general formula B so that the liquid crystal composition containing it has a higher clearing point, appropriate optical anisotropy, a larger absolute value of dielectric anisotropy, a larger K value, a lower residue concentration, a faster angular velocity, a smaller surface roughness of the polymer layer and a longer low-temperature storage time.

[0067] In some embodiments of the present invention, the weight percentage of the compound of general formula B in the liquid crystal composition is 0.1%-30% (including any numerical value or sub-range between the range), for example, 0.1%, 1%, 4%, 6%, 8%, 10%, 12%, 14%, 16%, 18%, 20%, 22%, 24%, 26%, 28%, 30%, or a range between any two values ​​therein; preferably, the weight percentage of the compound of general formula B in the liquid crystal composition is 0.1%-20%.

[0068] In some embodiments of the present invention, the compound of formula I is selected from the group consisting of:

[0069] as well as

[0070] In some embodiments of the present invention, in order to obtain a higher clearing point, appropriate optical anisotropy, a larger absolute value of dielectric anisotropy, a larger K value, a lower residue concentration, a faster angular velocity, better surface roughness of the polymer layer and a longer low-temperature storage time, the liquid crystal composition contains at least two (for example, 3, 4) compounds of general formula I; preferably, the liquid crystal composition contains at least one compound of general formula I-1 and at least one compound of general formula I-2.

[0071] In some embodiments of the present invention, preferably, R 11 and R 12 Each independently represents a straight chain or branched alkyl group containing 1 to 10 carbon atoms, a straight chain or branched alkoxy group containing 1 to 9 carbon atoms, or a straight chain or branched alkenyl group containing 2 to 10 carbon atoms; further preferably, R 11 and R 12 Each independently represents a straight chain or branched chain alkyl group containing 1 to 8 carbon atoms, a straight chain or branched chain alkoxy group containing 1 to 7 carbon atoms, or a straight chain or branched chain alkenyl group containing 2 to 8 carbon atoms.

[0072] In some embodiments of the present invention, R 11 represents a straight chain or branched chain alkyl group containing 1 to 8 carbon atoms, a straight chain or branched chain alkoxy group containing 1 to 7 carbon atoms, or a straight chain or branched chain alkenyl group containing 2 to 8 carbon atoms; R 12It represents a straight-chain or branched alkoxy group having 1 to 7 carbon atoms.

[0073] In some embodiments of the present invention, it is preferred to adjust the content of the compound of general formula I so that the liquid crystal composition of the present invention has a higher clearing point, appropriate optical anisotropy, a larger absolute value of dielectric anisotropy, a larger K value, a lower residue concentration, a faster angular velocity, a smaller surface roughness of the polymer layer and a longer low-temperature storage time.

[0074] In some embodiments of the present invention, the weight percentage of the compound of general formula I in the liquid crystal composition is 0.1%-40% (including any numerical value or sub-range between the range), for example, 0.1%, 0.5%, 1%, 2%, 4%, 6%, 8%, 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 20%, 22%, 24%, 25%, 26%, 28%, 30%, 32%, 34%, 35%, 36%, 38%, 40%, or a range between any two values ​​therein; preferably, the weight percentage of the compound of general formula I in the liquid crystal composition is 0.1%-35%.

[0075] In some embodiments of the present invention, the polymerizable compound of formula RM is selected from the group consisting of:

[0076]

[0077]

[0078]

[0079] as well as

[0080] in,

[0081] X1-X 10 , X 12 Each independently represents -F, -Cl, -Sp3-P3, a linear or branched alkyl or alkoxy group containing 1 to 5 carbon atoms,

[0082] In some embodiments of the present invention, X1-X 10 , X 12 Each independently represents -F, -Cl, -Sp3-P3, -CH3 or -OCH3.

[0083] In some embodiments of the present invention, Sp1 and Sp2 both represent single bonds.

[0084] In some embodiments of the present invention, in order to obtain an appropriate clearing point, an appropriate optical anisotropy, an appropriate absolute value of dielectric anisotropy, a larger K value, a smaller rotational viscosity, a lower residue concentration, a faster angular velocity, a smaller surface roughness of the polymer layer and a longer low-temperature storage time, the polymerizable compound of the general formula RM is selected from the group consisting of compounds of the general formula RM-1 and compounds of the general formula RM-2.

[0085] The polymerizable groups involved in the present invention are groups suitable for polymerization reactions (e.g., free radical or ionic polymerization, addition polymerization or condensation polymerization), or groups suitable for addition or condensation on the polymer backbone. For chain polymerization, polymerizable groups containing -C=C- or -C≡C- are particularly preferred, and for ring-opening polymerization, for example, oxetane or epoxy groups are particularly preferred.

[0086] In some embodiments of the present invention, the polymerizable groups P1, P2, P3, P 1 , P 2 , and P 3 Each independently expresses or -SH; preferably, the polymerizable groups P1, P2, P3, P 1 , P 2 , and P 3 Each independently expresses or -SH; further preferably, the polymerizable groups P1, P2, P3, P 1 , P 2 , and P 3 Each independently expresses

[0087] As used herein, the term "spacer group" is known to those skilled in the art and is described in the literature (e.g., Pure Appl. Chem. 2001, 73 (5), 888 and C. Tschierske, G. Pelzl, S. Diele, Angew. Chem. 2004, 116, 6340-6368). As used herein, the term "spacer group" refers to a flexible group that connects the mesogenic group and the polymerizable group in a polymerizable compound. Typical spacer groups are, for example, -(CH2)p1-, -(CH2CH2O)q1-CH2CH2-, -(CH2CH2S)q1-CH2CH2-, -(CH2CH2NH)q1-CH2CH2-, -CR 0 R 00 -(CH2) p1 -or-(SiR 0 R 00-O)p1-, wherein p1 represents an integer from 1 to 12 (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12), q1 represents an integer from 1 to 3 (e.g., 1, 2, 3), and R 0 and R 00 Each independently represents -H, a straight chain or branched alkyl group containing 1 to 12 (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12) carbon atoms, or a cyclic alkyl group containing 3 to 12 (e.g., 3, 4, 5, 6, 7, 8, 9, 10, 11, 12) carbon atoms. Particularly preferred spacer groups are -(CH2)p1-, -(CH2)p1-O-, -(CH2)p1-O-CO-, -(CH2)p1-CO-O-, -(CH2)p1-O-CO-O- or -CR 0 R 00 -(CH2) p1 -.

[0088] In some embodiments of the present invention, it is preferred to adjust the content of the polymerizable compound of the general formula RM so that the liquid crystal composition of the present invention has an appropriate clearing point, an appropriate optical anisotropy, an appropriate absolute value of dielectric anisotropy, a larger K value, a smaller rotational viscosity, a lower residue concentration, a faster angular velocity, a smaller surface roughness of the polymer layer and a longer low-temperature storage time.

[0089] In some embodiments of the present invention, the polymerizable compound of the general formula RM accounts for 0.001%-5% by weight of the liquid crystal composition (including any numerical value or sub-range between the ranges), for example, 0.001%, 0.002%, 0.004%, 0.005%, 0.006%, 0.008%, 0.01%, 0.02%, 0.04%, 0.06%, 0.08%, 0.1%, 0.2%, 0.25%, 0.26%, 0. 27%, 0.28%, 0.29%, 0.3%, 0.32%, 0.33%, 0.34%, 0.35%, 0.4%, 0.5%, 0.6%, 0.8%, 1%, 1.2%, 1.6%, 1.8%, 2%, 2.5%, 3%, 3.5%, 4%, 4.5%, 5%, or any range between two values; preferably, the weight percentage of the polymerizable compound of general formula RM in the liquid crystal composition is 0.001%-2%.

[0090] In some embodiments of the invention, Ls2 represents -Sp 3 -P 2 ,

[0091] In some embodiments of the invention, Sp 3 、Sp4 and Sp 5 Each independently represents -(CH2)p1-, -(CH2)p1-O-, -(CH2)p1-O-CO-, -(CH2)p1-CO-O-, -(CH2)p1-O-CO-O- or -CR 0 R 00 -(CH2) p1 -, wherein p1 represents an integer from 1 to 10 (e.g., 2, 3, 4, 5, 6, 7, 8 or 9), R 0 and R 00 Each independently represents -H or a linear or branched alkyl group containing 1 to 10 carbon atoms; preferably, in order to obtain a suitable clearing point, a suitable optical anisotropy, a suitable absolute value of dielectric anisotropy, a large K value, a low concentration of residues, a good pre-tilt angle stability and a small surface roughness of the polymer layer, Sp 3 、Sp 4 and Sp 5 Each independently represents -(CH2)p1- or -(CH2)p1-O-.

[0092] In some embodiments of the present invention, the self-aligning agent of formula SA is selected from the group consisting of the following compounds:

[0093]

[0094]

[0095] as well as

[0096] in,

[0097] LS 31 Indicates -F, -Cl, -CN, -NO2, -NCO, -NCS, -OCN, -SCN, -C(O)N(R S0 )2. -C(O)R S0 , a straight or branched alkyl group containing 1 to 12 (e.g., 2, 3, 4, 5, 6, 7, 8, 9, 10, or 11) carbon atoms, wherein one or more non-adjacent -CH2- in a straight-chain or branched alkyl group containing 1 to 12 carbon atoms can be independently replaced by -CH=CH-, -C≡C-, -O-, -CO-, -CO-O- or -O-CO-, and wherein a straight-chain or branched alkyl group containing 1 to 12 carbon atoms, One or more -H in the above-mentioned may be independently replaced by -F, wherein RS0 represents a straight or branched alkyl group containing 1 to 12 (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12) carbon atoms;

[0098] LS 21 Indicates -Sp 3 -P 2 or and

[0099] Z 11 Represents -O-, -S-, -CO-, -CO-O-, -O-CO-, -O-CO-O-, -CH2O-, -OCH2-, -CH2S-, -SCH2-, -CF2O-, -OCF2-, -CF2S-, -SCF2-, -(CH2) d -, -CF2CH2-, -CH2CF2-, -(CF2) d -, -CH=CH-, -CF=CF-, -CH=CF-, -CF=CH-, -C≡C-, -CH=CH-CO-O-, -O-CO-CH=CH-, -CH2CH2-CO-O-, -O-CO-CH2CH2-, -CHR 1 -、-CR 1 R 2 - or a single bond, where R 1 and R 2 Each independently represents a linear or branched alkyl group containing 1 to 12 carbon atoms, and d represents an integer of 1-4.

[0100] In some embodiments of the present invention, in order to obtain an appropriate clearing point, an appropriate optical anisotropy, an appropriate absolute value of dielectric anisotropy, a larger K value, a smaller rotational viscosity, a lower residue concentration, a faster angular velocity, a smaller surface roughness of the polymer layer and a longer low-temperature storage time, the compound of the general formula SA is selected from the group consisting of a compound of the general formula SA-1, a compound of the general formula SA-2, a compound of the general formula SA-3 and a compound of the general formula SA-21.

[0101] In some embodiments of the present invention, preferably, Ls1, Ls3 and Ls 31 Each independently represents -F, -Cl, -CN, -NO2, -NCO, -NCS, -OCN, -SCN, -C(O)N(R 0 )2. -C(O)R 0, a straight chain or branched chain alkyl group containing 1 to 10 carbon atoms, a straight chain or branched chain alkoxy group containing 1 to 9 carbon atoms, or a straight chain or branched chain alkenyl group containing 2 to 10 carbon atoms; further preferably, in order to obtain an appropriate clearing point, an appropriate optical anisotropy, an appropriate absolute value of dielectric anisotropy, a larger K value, a smaller rotational viscosity, a lower residue concentration, a faster angular velocity, a smaller surface roughness of the polymer layer, and a longer low temperature storage time Ls1, Ls3 and Ls 31 Each independently represents -F, -Cl, a straight-chain or branched alkyl group having 1 to 8 carbon atoms, a straight-chain or branched alkoxy group having 1 to 7 carbon atoms, or a straight-chain or branched alkenyl group having 2 to 8 carbon atoms.

[0102] In some embodiments of the present invention, preferably, R S1 Indicates Sp 1 -P 1 , a straight-chain or branched alkyl group containing 1 to 10 carbon atoms, a straight-chain or branched alkoxy group containing 1 to 9 carbon atoms, or a straight-chain or branched alkenyl group containing 2 to 10 carbon atoms; further preferably, R S1 It represents a straight chain or branched chain alkyl group having 1 to 8 carbon atoms, a straight chain or branched chain alkoxy group having 1 to 7 carbon atoms, and a straight chain or branched chain alkenyl group having 2 to 8 carbon atoms.

[0103] In some embodiments of the present invention, R S2 and R S3 Each independently represents -OH, -SH, -NH2, -NHR 11 、-N(R 11 )2. -NHC(O)R 11 、-OR 11 、-C(O)OH、

[0104] or *-X 1 .

[0105] In some embodiments of the present invention, R S2 and R S3 Each is independently selected from the group consisting of:

[0106] as well as

[0107] in,

[0108] * indicates the attachment site in the bonded structure.

[0109] In some embodiments of the present invention, in order to obtain an appropriate clearing point, an appropriate optical anisotropy, an appropriate absolute value of dielectric anisotropy, a larger K value, a smaller rotational viscosity, a lower residue concentration, a faster angle forming speed, a smaller surface roughness of the polymer layer and a longer low temperature storage time, R S2 and R S3 Each is independently selected from the group consisting of:

[0110] as well as

[0111] Furthermore, R S2 and R S3 Each independently preferably is: Furthermore, R S2 and R S3 Each independently preferably is: *-OH or

[0112] In some embodiments of the present invention, in order to obtain an appropriate clearing point, an appropriate optical anisotropy, an appropriate absolute value of dielectric anisotropy, a larger K value, a smaller rotational viscosity, a lower residue concentration, a faster angle forming speed, a smaller surface roughness of the polymer layer and a longer low temperature storage time, p s1 Indicates 1 or 2.

[0113] In some embodiments of the present invention, p s2 Represents 0 or 1.

[0114] In some embodiments of the present invention, the weight percentage of the compound of the general formula SA in the liquid crystal composition is 0.001% to 5% (including any value or sub-range between the range), for example, 0.001%, 0.005%, 0.05%, 0.1%, 0.2%, 0.25%, 0.3%, 0.35%, 0.4%, 0.45%, 0.5%, 0.55%, 0.6%, 0.65%, 0.7%, 0.75%, 0.8%, 0.85%, 0.9%, 0.95%, 1.0%, 2%, 3%, 4% or 5%, or a range between any two values ​​thereof; preferably, the weight percentage of the compound of the general formula SA in the liquid crystal composition is 0.1% to 2%.

[0115] In some embodiments of the present invention, the liquid crystal composition further comprises at least one compound of the general formula N:

[0116]

[0117] in,

[0118] R N1 and R N2 Each independently represents a straight or branched alkyl group containing 1 to 12 (e.g., 2, 3, 4, 5, 6, 7, 8, 9, 10, 11) carbon atoms, One or more non-adjacent -CH2- in the linear or branched alkyl group containing 1 to 12 carbon atoms may be independently replaced by -CH=CH-, -C≡C-, -O-, -CO-, -CO-O- or -O-CO-;

[0119] ring and ring Each independently expresses in One or more -CH2- in the ring may be replaced by -O-, and one or more single bonds in the ring may be replaced by double bonds, wherein One or more -H in the ring may be replaced by -F, -Cl or -CN, and one or more -CH= in the ring may be replaced by -N=;

[0120] Z N1 and Z N2 Each independently represents a single bond, -CO-O-, -O-CO-, -CH2O-, -OCH2-, -C≡C-, -CH=CH-, -CH2CH2- or -(CH2)4-;

[0121] L N1 and L N2 Each independently represents -H, an alkyl group containing 1 to 3 (e.g., 1, 2, 3) carbon atoms, or a halogen;

[0122] n N1 Represents 0, 1, 2, or 3, n N2 Represents 0 or 1, and 0≤n N1 +n N2 ≤3, when n N1 =2 or 3, the ring Can be the same or different, Z N1 Can be the same or different;

[0123] When n N1 +n N2 = 1, and the rings are connected by single bonds, the rings or ring Not for and

[0124] When n N1 =2,n N2 =0, and Z N1When all are single bonds, at least one ring Not for

[0125] In some embodiments of the present invention, L N1 and L N2 All represent -H.

[0126] In some embodiments of the present invention, the compound of formula N is selected from the group consisting of the following compounds:

[0127]

[0128]

[0129] as well as

[0130] In some embodiments of the present invention, preferably, R N1 and R N2 Each independently represents a straight chain or branched alkyl group containing 1 to 10 carbon atoms, a straight chain or branched alkoxy group containing 1 to 9 carbon atoms, or a straight chain or branched alkenyl group containing 2 to 10 carbon atoms; further preferably, R N1 and R N2 Each independently represents a straight chain or branched chain alkyl group containing 1 to 8 carbon atoms, a straight chain or branched chain alkoxy group containing 1 to 7 carbon atoms, or a straight chain or branched chain alkenyl group containing 2 to 8 carbon atoms.

[0131] In some embodiments of the present invention, the compound of general formula N is selected from the group consisting of compounds of general formula N-2, compounds of general formula N-6, compounds of general formula N-10, compounds of general formula N-13, compounds of general formula N-17, compounds of general formula N-19, compounds of general formula N-21, and compounds of general formula N-22.

[0132] In some embodiments of the present invention, in order to obtain an appropriate clearing point, appropriate optical anisotropy, a larger absolute value of dielectric anisotropy, a larger K value, a lower residue concentration, a faster angular velocity, a smaller surface roughness of the polymer layer and a longer low-temperature storage time, the compound of general formula N is selected from the group consisting of compounds of general formula N-2 and compounds of general formula N-10.

[0133] In some embodiments of the present invention, in order to obtain an appropriate clearing point, appropriate optical anisotropy, a larger absolute value of dielectric anisotropy, a larger K value, a lower residue concentration, a faster angular velocity, a smaller surface roughness of the polymer layer and a longer low-temperature storage time, the compound of general formula N is selected from the group consisting of compounds of general formula N-17 and compounds of general formula N-19; preferably, the liquid crystal composition contains at least two selected from the group consisting of compounds of general formula N-17 and compounds of general formula N-19; further preferably, the liquid crystal composition contains at least two compounds of general formula N-19.

[0134] In some embodiments of the present invention, in order to obtain an appropriate clearing point, appropriate optical anisotropy, a larger absolute value of dielectric anisotropy, a larger K value, a lower residue concentration, a faster angular velocity, a smaller surface roughness of the polymer layer and a longer low-temperature storage time, the compound of general formula N is selected from the group consisting of compounds of general formula N-21 and compounds of general formula N-22.

[0135] In some embodiments of the present invention, it is preferred to adjust the content of the compound of general formula N so that the liquid crystal composition of the present invention has an appropriate clearing point, an appropriate optical anisotropy, a larger absolute value of dielectric anisotropy, a larger K value, a lower residue concentration, a faster angular velocity, a smaller surface roughness of the polymer layer and a longer low-temperature storage time.

[0136] In some embodiments of the present invention, the weight percentage of the compound of general formula N in the liquid crystal composition is 0.1%-40% (including any numerical value or sub-range between the range), for example, 0.1%, 1%, 4%, 6%, 8%, 10%, 12%, 14%, 16%, 18%, 20%, 22%, 24%, 26%, 28%, 30%, 32%, 34%, 36%, 38%, 40%, or a range between any two values ​​therein; preferably, the weight percentage of the compound of general formula N in the liquid crystal composition is 0.1%-30%.

[0137] In some embodiments of the present invention, the liquid crystal composition comprises at least one compound of the general formula M:

[0138]

[0139] in,

[0140] R M1 and R M2 Each independently represents a straight or branched alkyl group containing 1 to 12 (e.g., 2, 3, 4, 5, 6, 7, 8, 9, 10, 11) carbon atoms, One or more non-adjacent -CH2- in the linear or branched alkyl group containing 1 to 12 carbon atoms may be independently replaced by -CH=CH-, -C≡C-, -O-, -CO-, -CO-O- or -O-CO-;

[0141] ring ring and ring Each independently expresses in One or more -CH2- in the ring may be replaced by -O-, one or more single bonds in the ring may be replaced by double bonds, At most one -H in may be replaced by halogen;

[0142] Z M1 and Z M2 Each independently represents a single bond, -CO-O-, -O-CO-, -CH2O-, -OCH2-, -C≡C-, -CH=CH-, -CH2CH2- or -(CH2)4-; and

[0143] n M represents 0, 1, or 2, where n M =2, ring Can be the same or different, Z M2 Can be the same or different.

[0144] In some embodiments of the present invention, preferably, R M1 and R M2 Each independently represents a straight chain or branched alkyl group containing 1 to 10 carbon atoms, a straight chain or branched alkoxy group containing 1 to 9 carbon atoms, or a straight chain or branched alkenyl group containing 2 to 10 carbon atoms; further preferably, R M1 and R M2 Each independently represents a straight chain or branched chain alkyl group containing 1 to 8 carbon atoms, a straight chain or branched chain alkoxy group containing 1 to 7 carbon atoms, or a straight chain or branched chain alkenyl group containing 2 to 8 carbon atoms.

[0145] In some embodiments of the present invention, R M1 and R M2 Preferably, each independently represents a straight chain alkenyl group containing 2 to 8 carbon atoms; R M1 and R M2 More preferably, each independently represents a straight-chain alkenyl group containing 2 to 5 carbon atoms.

[0146] In some embodiments of the present invention, preferably, R M1 and R M2One of them is a straight chain alkenyl group having 2 to 5 carbon atoms, and the other is a straight chain alkyl group having 1 to 5 carbon atoms.

[0147] In some embodiments of the present invention, preferably, R M1 and R M2 Each independently represents a straight chain alkoxy group containing 1 to 8 carbon atoms; further preferably, R M1 and R M2 Each independently represents a straight-chain alkoxy group containing 1 to 5 carbon atoms.

[0148] In some embodiments of the present invention, preferably, R M1 and R M2 One of them is a straight-chain alkoxy group having 1 to 5 carbon atoms, and the other is a straight-chain alkyl group having 1 to 5 carbon atoms.

[0149] In some embodiments of the present invention, when reliability is important, R M1 and R M2 are all alkyl groups; when it is important to reduce the volatility of the compound, R M1 and R M2 are alkoxy groups; when the viscosity reduction is important, R M1 and R M2 At least one of them is alkenyl.

[0150] The alkenyl group in the present invention is preferably selected from the group represented by any one of formula (V1) to formula (V9), and is particularly preferably formula (V1), formula (V2), formula (V8) or (V9). The groups represented by formula (V1) to formula (V9) are as follows:

[0151]

[0152] Here, * represents the carbon atom in the ring structure to which it is bonded.

[0153] The alkenyloxy group in the present invention is preferably selected from the group represented by any one of formula (OV1) to formula (OV9), and is particularly preferably the group represented by formula (OV1), formula (OV2), formula (OV8) or (OV9). The groups represented by formula (OV1) to formula (OV9) are as follows:

[0154]

[0155] Here, * represents the carbon atom in the ring structure to which it is bonded.

[0156] In some embodiments of the present invention, the compound of formula M is selected from the group consisting of:

[0157]

[0158]

[0159] as well as

[0160] In some embodiments of the present invention, in order to obtain an appropriate clearing point, appropriate optical anisotropy, a larger K value, a smaller rotational viscosity, a smaller residue concentration, a faster angular velocity, a smaller surface roughness of the polymer layer and a longer low-temperature storage time, the compound of general formula M is selected from the group consisting of compounds of general formula M-1, compounds of general formula M-4, compounds of general formula M-11, and compounds of general formula M-13; preferably, the liquid crystal composition contains at least two compounds of general formula M.

[0161] In some embodiments of the present invention, the content of the compound of formula M must be appropriately adjusted according to the required properties such as solubility at low temperature, transition temperature, electrical reliability, birefringence, process adaptability, drip marks, screen burn-in, dielectric anisotropy, etc.

[0162] In some embodiments of the present invention, it is preferred to adjust the content of the compound of the general formula M so that the liquid crystal composition of the present invention has an appropriate clearing point, appropriate optical anisotropy, a larger K value, a smaller rotational viscosity, a smaller residue concentration, a faster angular velocity, a smaller polymer layer surface roughness and a longer low-temperature storage time.

[0163] In some embodiments of the present invention, the weight percentage of the compound of general formula M in the liquid crystal composition is 0.1%-60% (including any numerical value or sub-range between this range), for example, 0.1%, 1%, 4%, 6%, 8%, 10%, 12%, 14%, 16%, 18%, 20%, 22%, 24%, 26%, 28%, 30%, 32%, 34%, 36%, 38%, 40%, 42%, 44%, 46%, 48%, 50%, 52%, 54%, 56%, 58%, 60%, or the range between any two values.

[0164] In some embodiments of the present invention, the liquid crystal composition of the present invention further comprises at least one compound selected from the group consisting of compounds of formula A-1 and formula A-2

[0165]

[0166] in,

[0167] R A1 and R A2Each independently represents a straight or branched alkyl group containing 1 to 12 (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12) carbon atoms, One or more non-adjacent -CH2- in the straight-chain or branched alkyl group containing 1 to 12 carbon atoms can be independently replaced by -CH=CH-, -C≡C-, -O-, -CO-, -CO-O- or -O-CO-, and the straight-chain or branched alkyl group containing 1 to 12 carbon atoms, One or more -H in can be independently replaced by -F or -Cl;

[0168] ring ring ring and ring Each independently expresses in One or more -CH2- in the ring may be replaced by -O-, and one or more single bonds in the ring may be replaced by double bonds, wherein One or more -H in the ring may be replaced by -F, -Cl or -CN, and one or more -CH= in the ring may be replaced by -N=;

[0169] Z A11 , Z A21 and Z A22 each independently represents a single bond, -CH2CH2-, -CF2CF2-, -CO-O-, -O-CO-, -O-CO-O-, -CH=CH-, -CF=CF-, -CH2O- or -OCH2-;

[0170] L A11 , L A12 , L A13 , L A21 and L A22 Each independently represents -H, an alkyl group containing 1 to 3 carbon atoms or a halogen;

[0171] X A1 and X A2 Each independently represents halogen, a haloalkyl or haloalkoxy group containing 1 to 5 carbon atoms, a haloalkenyl or haloalkenyloxy group containing 2 to 5 carbon atoms;

[0172] n A11 Represents 0, 1, 2, or 3. When n A11 =2 or 3, the ring Can be the same or different, Z A11 Can be the same or different;

[0173] n A12 represents 1 or 2, where nA12 =2, ring may be the same or different; and

[0174] n A2 represents 0, 1, 2, or 3, where n A2 =2 or 3, the ring Can be the same or different, Z A21 Can be the same or different.

[0175] In some embodiments of the present invention, the compound of formula A-1 is selected from the group consisting of the following compounds:

[0176]

[0177] as well as

[0178] in,

[0179] R A1 represents a straight or branched alkyl group containing 1 to 8 carbon atoms, One or more non-adjacent -CH2- in the linear or branched alkyl group containing 1 to 8 carbon atoms may be independently replaced by -CH=CH-, -C≡C-, -O-, -CO-, -CO-O- or -O-CO-, and one or more -H in these groups may be independently replaced by -F or -Cl;

[0180] R v and R w Each independently represents -CH2- or -O-;

[0181] L A11 , L A12 , L A11 ', L A12 ', L A14 , L A15 and L A16 Each independently represents -H or -F;

[0182] L A13 and L A13 'Each independently represents -H or -CH3;

[0183] X A1 represents -F, -CF3 or -OCF3; and

[0184] v and w each independently represent 0 or 1.

[0185] In some embodiments of the present invention, the weight percentage of the compound of general formula A-1 in the liquid crystal composition is 0.1%-50% (including any value or sub-range between the range), for example, 0.1%, 1%, 4%, 6%, 8%, 10%, 12%, 14%, 16%, 18%, 20%, 22%, 24%, 26%, 28%, 30%, 32%, 34%, 36%, 38%, 40%, 42%, 44%, 46%, 48%, 50%, or a range between any two values.

[0186] Regarding the preferred content of the compound of general formula A-1, when the viscosity of the liquid crystal composition of the present invention is kept low and the response speed is fast, it is preferred to make its lower limit value slightly lower and the upper limit value slightly lower; further, when the clearing point of the liquid crystal composition of the present invention is kept high and the temperature stability is good, it is preferred to make its lower limit value slightly lower and the upper limit value slightly lower; in addition, in order to keep the driving voltage low and increase the absolute value of dielectric anisotropy, it is preferred to make its lower limit value slightly higher and the upper limit value slightly higher.

[0187] In some embodiments of the present invention, the compound of formula A-2 is selected from the group consisting of:

[0188]

[0189] as well as

[0190] in,

[0191] R A2 represents a straight-chain or branched alkyl group containing 1 to 8 carbon atoms, wherein one or more non-adjacent -CH2- groups in the straight-chain or branched alkyl group containing 1 to 8 carbon atoms may be independently replaced by -CH=CH-, -C≡C-, -O-, -CO-, -CO-O- or -O-CO-, and one or more -H groups in these groups may be independently replaced by -F or -Cl;

[0192] L A21 , L A22 , L A23 , L A24 and L A25 each independently represents -H or -F; and

[0193] X A2 It represents -F, -CF3, -OCF3 or -CH2CH2CH=CF2.

[0194] In some embodiments of the present invention, the weight percentage of the compound of general formula A-2 in the liquid crystal composition is 0.1%-50% (including any numerical value or sub-range between the range), for example, 0.1%, 1%, 4%, 6%, 8%, 10%, 12%, 14%, 16%, 18%, 20%, 22%, 24%, 26%, 28%, 30%, 32%, 34%, 36%, 38%, 40%, 42%, 44%, 46%, 48%, 50%, or a range between any two of the numerical values.

[0195] Regarding the preferred content of the compound of general formula A-2, when the viscosity of the liquid crystal composition of the present invention is kept low and the response speed is fast, it is preferred to make its lower limit value slightly lower and the upper limit value slightly lower; further, when the clearing point of the liquid crystal composition of the present invention is kept high and the temperature stability is good, it is preferred to make its lower limit value slightly lower and the upper limit value slightly lower; in addition, in order to keep the driving voltage low and increase the absolute value of the dielectric anisotropy, it is preferred to make its lower limit value slightly higher and the upper limit value slightly higher.

[0196] In some embodiments of the present invention, the liquid crystal composition comprises at least one additive.

[0197] In addition to the above compounds, the liquid crystal composition of the present invention may also contain conventional nematic liquid crystals, smectic liquid crystals, cholesteric liquid crystals, dopants, antioxidants, ultraviolet absorbers, infrared absorbers, polymerizable monomers or light stabilizers.

[0198] Possible dopants which are preferably added to the liquid crystal composition according to the invention are shown below:

[0199]

[0200] as well as

[0201] In some embodiments of the present invention, the weight percentage of the dopant in the liquid crystal composition is 0%-5%; preferably, the weight percentage of the dopant in the liquid crystal composition is 0.01%-1%.

[0202] In addition, the antioxidant, light stabilizer, ultraviolet absorber and other additives used in the liquid crystal composition of the present invention are preferably the following:

[0203]

[0204]

[0205]

[0206] Here, n represents a positive integer from 1 to 12.

[0207] Preferably, the antioxidant is selected from the light stabilizers shown below:

[0208]

[0209] In some embodiments of the present invention, the additive accounts for 0%-5% of the total weight of the liquid crystal composition; preferably, the additive accounts for 0.01%-1% of the total weight of the liquid crystal composition.

[0210] In yet another aspect, the present invention further provides a liquid crystal display device, comprising the liquid crystal composition.

[0211] In some embodiments of the present invention, the liquid crystal composition is particularly suitable for use in PSA-VA, PSA-OCB, PSA-IPS, PSA-FFS and PSA-TN type liquid crystal display elements.

[0212] As used herein, the terms "tilt" and "tilt angle" are to be understood as the tilted alignment of the liquid crystal molecules relative to the surface of the liquid crystal cell in a liquid crystal display device (preferably, a PSA type liquid crystal display device). The tilt angle represents the average angle (<90°) formed between the longitudinal molecular axes (liquid crystal director) of the liquid crystal molecules and the surface of the outer plate of the liquid crystal cell. A low value of the tilt angle (i.e., a large angle deviating from 90°) corresponds to a large tilt.

[0213] Beneficial effects: Compared with the prior art, the liquid crystal composition of the present invention has a higher clearing point, a proper optical anisotropy, a larger absolute value of dielectric anisotropy, and a larger K value (K 11 Value, K 33 The present invention discloses a liquid crystal display device comprising the liquid crystal composition. The liquid crystal display device has a lower residual concentration after applying UV2 for 90 min under the condition of lower rotational viscosity and lower rotational viscosity, and has a faster angular velocity, a smaller surface roughness of the polymer layer, and a longer low-temperature storage time under the same time. Therefore, the liquid crystal display device comprising the liquid crystal composition has better contrast, faster response speed, and vertical alignment of liquid crystal molecules without a PI alignment layer while maintaining a wider temperature use range and a smaller threshold voltage. The liquid crystal display device can effectively accelerate the production process of PSA liquid crystal displays and improve production efficiency. Meanwhile, the problems of "image viscosity", uneven display, and "broken bright spots" existing in existing PSA liquid crystal displays can be effectively improved, and the liquid crystal display device has a higher practical application value. DETAILED DESCRIPTION

[0214] The present invention will be described below in conjunction with specific embodiments. It should be noted that the following embodiments are examples of the present invention and are only used to illustrate the present invention, but not to limit the present invention. Other combinations and various modifications within the concept of the present invention may be performed without departing from the spirit or scope of the present invention.

[0215] For ease of expression, in the following examples, the group structure of each compound is represented by the code listed in Table 1:

[0216] Table 1. Group structure codes of compounds

[0217]

[0218]

[0219] Take the following compound as an example:

[0220]

[0221] If the structural formula is represented by the codes listed in Table 2, it can be expressed as: nCCGF, where n in the code represents the number of C atoms in the left-end alkyl group, for example, n is "3", which means that the alkyl group is -C3H7; C in the code represents 1,4-cyclohexylene, G represents 2-fluoro-1,4-phenylene, and F represents fluorine.

[0222] The abbreviated codes for the test items in the following embodiments are as follows:

[0223] Cp clearing point (nematic-isotropic phase transition temperature, °C)

[0224] Δn optical anisotropy (589nm, 20℃)

[0225] Δε Dielectric anisotropy (1KHz, 20℃)

[0226] K 11 Splay elastic constant (20℃)

[0227] K 33 Bending elastic constant (20℃)

[0228] γ1 Rotational viscosity (mPa·s, 20℃)

[0229] Ra Roughness(nm)

[0230] PTA pre-tilt angle (°, 20°C)

[0231] t (-10℃) Low temperature storage time (days, -10℃)

[0232] in,

[0233] Cp: ​​obtained by melting point test.

[0234] Δn: measured using an Abbe refractometer under a sodium lamp (589 nm) at 20°C.

[0235] Δε:Δε=ε ∥ -ε ⊥ , where ε ∥ is the dielectric constant parallel to the molecular axis, ε ⊥ is the dielectric constant perpendicular to the molecular axis; test conditions: 20°C, 1KHz, VA type test box with a box thickness of 6μm.

[0236] γ1: obtained by testing using LCM-2 liquid crystal property evaluation system; test conditions: 20°C, 160-260V, test box thickness 20μm.

[0237] K 11 and K 33 : The CV curve of the liquid crystal is tested and calculated using an LCR meter and a VA test box; test conditions: box thickness 6μm, V=0.1~20V.

[0238] Ra: After a liquid crystal composition containing a polymerizable compound is polymerized by UV light, the liquid crystal molecules are washed away, and then an atomic force microscope (AFM) is used to test the morphology roughness of the polymer layer after polymerization.

[0239] PTA: Using the crystal rotation method, the liquid crystal was poured into a VA test box (box thickness 3.5 μm), a voltage (15 V, 60 Hz) was applied, and UV light UV1 (5.5 mw / cm -2 , 313nm) to irradiate the polymerizable compound to form a pre-tilt angle PTA1, and then continue to irradiate the liquid crystal composition having formed a pre-tilt angle PTA1 with ultraviolet light UV2 (0.25mw / cm -2 , 313nm) to eliminate the residual polymerizable compound in the PTA1 state, and the pre-tilt angle formed by the polymerizable compound at this time is PTA2. The present invention examines the polymerization speed of the polymerizable compound by comparing the size of the pre-tilt angle formed when UV1 is irradiated for the same time (the smaller the pre-tilt angle, the faster the polymerization speed) or comparing the time required to form the same pre-tilt angle (the shorter the time required, the faster the polymerization speed).

[0240] Residue concentration: After applying UV2 irradiation for 90 min, the liquid crystal eluted from the liquid crystal test box was detected by high performance liquid chromatography (HPLC), and the content of polymerizable compounds and self-alignment agents therein was called the residue concentration.

[0241] t (-10℃): The nematic liquid crystal medium is placed in a glass bottle and stored at -10°C, and the time is recorded when crystal precipitation is observed.

[0242] Each component used in the following examples can be synthesized by a known method or obtained through commercial channels. These synthesis techniques are conventional, and each liquid crystal compound obtained meets the standards of electronic compounds after testing.

[0243] Liquid crystal compositions are prepared according to the ratios of the liquid crystal compositions specified in the following examples. The preparation of the liquid crystal compositions is carried out according to conventional methods in the art, such as mixing in proportion by heating, ultrasonic waves, suspension, etc.

[0244] The structures of the polymerizable compounds used in the following examples are shown in Table 2:

[0245] Table 2. Structure, component number and code of polymerizable compounds

[0246]

[0247] The structures of the self-aligning agents used in the following examples are shown in Table 3:

[0248] Table 3. Structure, component number and code of self-aligning agent

[0249]

[0250]

[0251]

[0252] Liquid crystal compositions of control Host-1, Host-1 and Host-2 were prepared according to the compounds and their weight percentages listed in Table 4, and filled between two substrates of a liquid crystal display for performance testing.

[0253] Table 4 Liquid crystal composition formula and performance parameter test results

[0254]

[0255] Liquid crystal compositions of Host-2 and Host-3 were prepared according to the compounds and their weight percentages listed in Table 5, and filled between two substrates of a liquid crystal display for performance testing.

[0256] Table 5 Formulation and performance parameter test results of liquid crystal composition

[0257]

[0258] Liquid crystal compositions of Host-3 and Host-4 were prepared according to the compounds and their weight percentages listed in Table 6, and filled between two substrates of a liquid crystal display for performance testing.

[0259] Table 6 Formulation and performance parameter test results of liquid crystal composition

[0260]

[0261]

[0262] Liquid crystal compositions of Host-4 and Host-5 were prepared according to the compounds and their weight percentages listed in Table 7, and filled between two substrates of a liquid crystal display for performance testing.

[0263] Table 7 Formulation and performance parameter test results of liquid crystal composition

[0264]

[0265] Liquid crystal compositions of Host-5 and Host-6 were prepared according to the compounds and their weight percentages listed in Table 8, and filled between two substrates of a liquid crystal display for performance testing.

[0266] Table 8 Formulation and performance parameter test results of liquid crystal composition

[0267]

[0268]

[0269] 0.3 parts by weight of polymerizable compound RM-01 and 0.6 parts by weight of Add-1 were added to 100 parts by weight of liquid crystal composition control Host-1. As comparative example 1, 0.3 parts by weight of polymerizable compound RM-01 and 0.6 parts by weight of Add-1 were added to 100 parts by weight of liquid crystal compositions Host-1 and Host-2. As examples 1-2, the obtained liquid crystal compositions were filled into a "non-aligned" test box (the box thickness d was 3.5 μm, with ITO coating on both sides (structured ITO in the case of multi-domain switching), no alignment layer and no passivation layer), and the relevant performance test results are shown in Table 9 below:

[0270] Table 9 Specific weight fractions of polymerizable compounds and related performance test results

[0271]

[0272] From the comparison between Examples 1-2 and Comparative Example 1, it can be seen that the present invention comprises at least two compounds of the general formula B, at least one compound of the general formula II, a polymerizable compound RM and a self-aligning agent of the general formula SA, so that the liquid crystal composition of the present invention maintains a high clearing point, a suitable optical anisotropy, a large absolute value of dielectric anisotropy, and a suitable K value (K 11 Value, K 33 value) and appropriate rotational viscosity, the residue concentration after applying UV2 for 90 min is lower, and at the same time, it has a faster angular velocity, smaller surface roughness of the polymer layer and a longer low-temperature storage time.

[0273] 0.3 parts by weight of the polymerizable compound RM-01 and 0.6 parts by weight of Add-2 were added to 100 parts by weight of the liquid crystal composition control Host-1. As comparative example 2, 0.3 parts by weight of the polymerizable compound RM-01 and 0.6 parts by weight of Add-2 were added to 100 parts by weight of the liquid crystal compositions Host-1 and Host-2. As examples 3-4, the obtained liquid crystal compositions were filled into a "non-aligned" test box (the box thickness d was 3.5 μm, with an ITO coating on both sides (structured ITO in the case of multi-domain switching), no alignment layer and no passivation layer), and the relevant performance test results are shown in Table 10 below:

[0274] Table 10 Specific weight fractions of polymerizable compounds and related performance test results

[0275]

[0276] From the comparison between Examples 3-4 and Comparative Example 2, it can be seen that the present invention comprises at least two compounds of the general formula B, at least one compound of the general formula II, a polymerizable compound RM and a self-aligning agent of the general formula SA, so that the liquid crystal composition of the present invention maintains a high clearing point, a suitable optical anisotropy, a large absolute value of dielectric anisotropy, and a suitable K value (K 11 Value, K 33 value) and appropriate rotational viscosity, the residue concentration after applying UV2 for 90 min is lower, and at the same time, it has a faster angular velocity, smaller surface roughness of the polymer layer and a longer low-temperature storage time.

[0277] 0.3 parts by weight of the polymerizable compound RM-01 and 0.6 parts by weight of Add-3 were added to 100 parts by weight of the liquid crystal composition control Host-2. As comparative example 3, 0.3 parts by weight of the polymerizable compound RM-01 and 0.6 parts by weight of Add-3 were added to 100 parts by weight of the liquid crystal composition Host-3. As example 5, the obtained liquid crystal composition was filled into a "non-aligned" test box (the box thickness d was 3.5 μm, with ITO coating on both sides (structured ITO in the case of multi-domain switching), no alignment layer and no passivation layer), and the relevant performance test results are shown in Table 11 below:

[0278] Table 11 Specific weight fractions of polymerizable compounds and related performance test results

[0279]

[0280] From the comparison between Example 5 and Comparative Example 3, it can be seen that the present invention comprises at least two compounds of the general formula B, at least one compound of the general formula II, a polymerizable compound RM and a self-aligning agent of the general formula SA, so that the liquid crystal composition of the present application maintains an appropriate clearing point, an appropriate optical anisotropy, a large absolute value of dielectric anisotropy, and an appropriate K value (K 11 Value, K 33 value) and appropriate rotational viscosity, the residue concentration after applying UV2 for 90 min is lower, and at the same time, it has a faster angular velocity, smaller surface roughness of the polymer layer and a longer low-temperature storage time.

[0281] 0.3 parts by weight of polymerizable compound RM-01 and 0.6 parts by weight of Add-5 were added to 100 parts by weight of liquid crystal composition control Host-2. As comparative example 4, 0.3 parts by weight of polymerizable compound RM-01 and 0.6 parts by weight of Add-5 were added to 100 parts by weight of liquid crystal composition Host-3. As example 6, the obtained liquid crystal composition was filled into a "non-aligned" test box (the box thickness d was 3.5 μm, with ITO coating on both sides (structured ITO in the case of multi-domain switching), no alignment layer and no passivation layer), and the relevant performance test results are shown in Table 12 below:

[0282] Table 12 Specific weight fractions of polymerizable compounds and related performance test results

[0283]

[0284] From the comparison between Example 6 and Comparative Example 4, it can be seen that the present invention comprises at least two compounds of the general formula B, at least one compound of the general formula II, a polymerizable compound RM and a self-aligning agent of the general formula SA, so that the liquid crystal composition of the present application maintains an appropriate clearing point, an appropriate optical anisotropy, a large absolute value of dielectric anisotropy, and an appropriate K value (K 11 Value, K 33 value) and appropriate rotational viscosity, the residue concentration after applying UV2 for 90 min is lower, and at the same time, it has a faster angular velocity, smaller surface roughness of the polymer layer and a longer low-temperature storage time.

[0285] 0.3 parts by weight of polymerizable compound RM-02 and 0.6 parts by weight of Add-1 were added to 100 parts by weight of liquid crystal composition control Host-3. As comparative example 5, 0.3 parts by weight of polymerizable compound RM-02 and 0.6 parts by weight of Add-1 were added to 100 parts by weight of liquid crystal composition Host-4. As example 7, the obtained liquid crystal composition was filled into a "non-aligned" test box (the box thickness d was 3.5 μm, with ITO coating on both sides (structured ITO in the case of multi-domain switching), no alignment layer and no passivation layer), and the relevant performance test results are shown in Table 13 below:

[0286] Table 13 Specific weight fractions of polymerizable compounds and related performance test results

[0287]

[0288]

[0289] From the comparison between Example 7 and Comparative Example 5, it can be seen that the present invention comprises at least two compounds of the general formula B, at least one compound of the general formula II, a polymerizable compound RM and a self-aligning agent of the general formula SA, so that the liquid crystal composition of the present application maintains an appropriate clearing point, an appropriate optical anisotropy, an appropriate absolute value of dielectric anisotropy, a larger K value (K 11 Value, K 33 value) and smaller rotational viscosity, the residue concentration after applying UV2 for 90 min is lower, and at the same time, it has a faster angular velocity, smaller surface roughness of the polymer layer and a longer low-temperature storage time.

[0290] 0.3 parts by weight of the polymerizable compound RM-02 and 0.6 parts by weight of Add-2 were added to 100 parts by weight of the liquid crystal composition control Host-3. As comparative example 6, 0.3 parts by weight of the polymerizable compound RM-02 and 0.6 parts by weight of Add-2 were added to 100 parts by weight of the liquid crystal composition Host-4. As example 8, the obtained liquid crystal composition was filled into a "non-aligned" test box (the box thickness d was 3.5 μm, with ITO coating on both sides (structured ITO in the case of multi-domain switching), no alignment layer and no passivation layer), and the relevant performance test results are shown in Table 14 below:

[0291] Table 14 Specific weight fractions of polymerizable compounds and related performance test results

[0292]

[0293] From the comparison between Example 8 and Comparative Example 4, it can be seen that the present invention comprises at least two compounds of the general formula B, at least one compound of the general formula II, a polymerizable compound RM and a self-aligning agent of the general formula SA, so that the liquid crystal composition of the present application maintains an appropriate clearing point, an appropriate optical anisotropy, an appropriate absolute value of dielectric anisotropy, a larger K value (K 11 Value, K 33 value) and smaller rotational viscosity, the residue concentration after applying UV2 for 90 min is lower, and at the same time, it has a faster angular velocity, smaller surface roughness of the polymer layer and a longer low-temperature storage time.

[0294] 0.3 parts by weight of polymerizable compound RM-02 and 0.6 parts by weight of Add-3 were added to 100 parts by weight of liquid crystal composition control Host-4. As comparative example 7, 0.3 parts by weight of polymerizable compound RM-02 and 0.6 parts by weight of Add-3 were added to 100 parts by weight of liquid crystal composition Host-5. As example 9, the obtained liquid crystal composition was filled into a "non-aligned" test box (the box thickness d was 3.5 μm, with ITO coating on both sides (structured ITO in the case of multi-domain switching), no alignment layer and no passivation layer), and the relevant performance test results are shown in Table 15 below:

[0295] Table 15 Specific weight fractions of polymerizable compounds and related performance test results

[0296]

[0297] From the comparison between Example 9 and Comparative Example 7, it can be seen that the present invention comprises at least two compounds of the general formula B, at least one compound of the general formula II, a polymerizable compound RM and a self-aligning agent of the general formula SA, so that the liquid crystal composition of the present application maintains an appropriate clearing point, an appropriate optical anisotropy, an appropriate absolute value of dielectric anisotropy, a larger K value (K 11 Value, K 33 value) and smaller rotational viscosity, the residue concentration after applying UV2 for 90 min is lower, and at the same time, it has a faster angular velocity, smaller surface roughness of the polymer layer and a longer low-temperature storage time.

[0298] 0.3 parts by weight of the polymerizable compound RM-02 and 0.6 parts by weight of Add-5 were added to 100 parts by weight of the liquid crystal composition control Host-4. As comparative example 8, 0.3 parts by weight of the polymerizable compound RM-02 and 0.6 parts by weight of Add-5 were added to 100 parts by weight of the liquid crystal composition Host-5. As example 10, the obtained liquid crystal composition was filled into a "non-aligned" test box (the box thickness d was 3.5 μm, with ITO coating on both sides (structured ITO in the case of multi-domain switching), no alignment layer and no passivation layer), and the relevant performance test results are shown in Table 16 below:

[0299] Table 16 Specific weight fractions of polymerizable compounds and related performance test results

[0300]

[0301] From the comparison between Example 10 and Comparative Example 8, it can be seen that the present invention comprises at least two compounds of the general formula B, at least one compound of the general formula II, a polymerizable compound RM and a self-aligning agent of the general formula SA, so that the liquid crystal composition of the present application maintains an appropriate clearing point, an appropriate optical anisotropy, an appropriate absolute value of dielectric anisotropy, a larger K value (K 11 Value, K 33 value) and smaller rotational viscosity, the residue concentration after applying UV2 for 90 min is lower, and at the same time, it has a faster angular velocity, smaller surface roughness of the polymer layer and a longer low-temperature storage time.

[0302] 0.3 parts by weight of polymerizable compound RM-01 and 0.3 parts by weight of Add-4 were added to 100 parts by weight of liquid crystal composition control Host-5. As comparative example 9, 0.3 parts by weight of polymerizable compound RM-01 and 0.3 parts by weight of Add-4 were added to 100 parts by weight of liquid crystal composition Host-6. As example 11, the obtained liquid crystal composition was filled into a "non-aligned" test box (the box thickness d was 3.5 μm, with ITO coating on both sides (structured ITO in the case of multi-domain switching), no alignment layer and no passivation layer), and the relevant performance test results are shown in Table 17 below:

[0303] Table 17 Specific weight fractions of polymerizable compounds and related performance test results

[0304]

[0305] From the comparison between Example 11 and Comparative Example 9, it can be seen that the present invention comprises at least two compounds of the general formula B, at least one compound of the general formula II, a polymerizable compound RM and a self-aligning agent of the general formula SA, so that the liquid crystal composition of the present application maintains a high clearing point, a suitable optical anisotropy, a large absolute value of dielectric anisotropy, and a suitable K value (K 11 Value, K 33 value) and appropriate rotational viscosity, the residue concentration after applying UV2 for 90 min is lower, and at the same time, it has a faster angular velocity, smaller surface roughness of the polymer layer and a longer low-temperature storage time.

[0306] 0.3 parts by weight of the polymerizable compound RM-01 and 0.6 parts by weight of Add-6 were added to 100 parts by weight of the liquid crystal composition control Host-5. As comparative example 10, 0.3 parts by weight of the polymerizable compound RM-01 and 0.6 parts by weight of Add-6 were added to 100 parts by weight of the liquid crystal composition Host-6. As example 12, the obtained liquid crystal composition was filled into a "non-aligned" test box (the box thickness d was 3.5 μm, with ITO coating on both sides (structured ITO in the case of multi-domain switching), no alignment layer and no passivation layer), and the relevant performance test results are shown in Table 18 below:

[0307] Table 18 Specific weight fractions of polymerizable compounds and related performance test results

[0308]

[0309] From the comparison between Example 12 and Comparative Example 10, it can be seen that the present invention comprises at least two compounds of the general formula B, at least one compound of the general formula II, a polymerizable compound RM and a self-aligning agent of the general formula SA, so that the liquid crystal composition of the present application maintains a high clearing point, a suitable optical anisotropy, a large absolute value of dielectric anisotropy, and a suitable K value (K 11 Value, K 33 value) and appropriate rotational viscosity, the residue concentration after applying UV2 for 90 min is lower, and at the same time, it has a faster angular velocity, smaller surface roughness of the polymer layer and a longer low-temperature storage time.

[0310] In summary, the liquid crystal composition of the present invention has high clearing point, appropriate optical anisotropy, large absolute value of dielectric anisotropy, large K value (K 11 Value, K 33 The present invention discloses a liquid crystal display device comprising the liquid crystal composition. The liquid crystal display device has a lower residual concentration after applying UV2 for 90 min under the condition of lower rotational viscosity and lower rotational viscosity, and has a faster angular velocity, a smaller surface roughness of the polymer layer, and a longer low-temperature storage time under the same time. Therefore, the liquid crystal display device comprising the liquid crystal composition has better contrast, faster response speed, and vertical alignment of liquid crystal molecules without a PI alignment layer while maintaining a wider temperature use range and a smaller threshold voltage. The liquid crystal display device can effectively accelerate the production process of PSA liquid crystal displays and improve production efficiency. Meanwhile, the problems of "image viscosity", uneven display, and "broken bright spots" existing in existing PSA liquid crystal displays can be effectively improved, and the liquid crystal display device has a higher practical application value.

[0311] The above implementation modes are only for illustrating the technical concept and features of the present invention, and their purpose is to enable people familiar with this technology to understand the content of the present invention and implement it, and they cannot be used to limit the protection scope of the present invention. Any equivalent changes or modifications made according to the spirit of the present invention should be included in the protection scope of the present invention.

Claims

1. A liquid crystal composition, characterized in that: The liquid crystal composition comprises: At least two compounds of formula B At least one compound of formula I, wherein the compound of formula I is selected from the group consisting of the following compounds: At least one polymerizable compound of the general formula RM At least one self-aligning agent of the general formula SA At least one compound of the general formula N At least one compound of the general formula M in, R B1 and R B2 Each independently represents halogen, -CF3, -OCF3, a straight or branched alkyl group containing 1 to 12 carbon atoms, The straight or branched alkyl group containing 1 to 12 carbon atoms, One or more non-adjacent -CH2- in the above mentioned group may be independently replaced by -O-, -S-, -CH=CH-, -C≡C-, -CO-, -CO-O- or -O-CO-, and one or more -H in the straight or branched alkyl group containing 1 to 12 carbon atoms may be independently replaced by -F or -Cl; R 11 and R 12 Each independently represents a straight-chain or branched alkyl group containing 1 to 12 carbon atoms, and one or more non-adjacent -CH2- in the straight-chain or branched alkyl group containing 1 to 12 carbon atoms can be independently replaced by -C=C-, -C≡C-, -O-, -CO-, -CO-O- or -O-CO-; R1 represents -H, halogen, -CN, -Sp2-P2, a straight or branched alkyl group containing 1 to 12 carbon atoms, wherein the straight or branched alkyl group containing 1 to 12 carbon atoms, One or more non-adjacent -CH2- may be independently replaced by -CH=CH-, -C≡C-, -O-, -CO-, -CO-O- or -O-CO-, and one or more -H may be independently replaced by -F or -Cl; R S1 Indicates -Sp 1 -P 1 , a straight or branched alkyl group containing 1 to 12 carbon atoms, wherein one or more non-adjacent -CH2- in a straight-chain or branched alkyl group containing 1 to 12 carbon atoms can be independently replaced by -CH=CH-, -C≡C-, -O-, -CO-, -CO-O- or -O-CO-, and wherein a straight-chain or branched alkyl group containing 1 to 12 carbon atoms, One or more -H in can be independently replaced by -F or -Cl; ring and ring Each independently expresses in One or more -CH2- in the ring may be replaced by -O-, and one or more single bonds in the ring may be replaced by double bonds, wherein One or more -H in the ring may be independently replaced by -CN, -F or -Cl, and one or more -CH= in the ring may be replaced by -N=; ring and ring Each independently expresses in One or more -CH2- in the ring may be replaced by -O-, and one or more single bonds in the ring may be replaced by double bonds, wherein One or more -H in the group may be replaced independently by -F, -Cl, -CN, -Sp3-P3, a halogenated or unhalogenated straight-chain alkyl group containing 1 to 12 carbon atoms, a halogenated or unhalogenated straight-chain alkoxy group containing 1 to 11 carbon atoms, substituted, and -CH= in one or more rings may be replaced by -N=; ring express in One or more -H in the group may be independently replaced by -F, -Cl, -CN, -Sp3-P3, a halogenated or unhalogenated straight-chain alkyl group containing 1 to 12 carbon atoms, a halogenated or unhalogenated straight-chain alkoxy group containing 1 to 11 carbon atoms, substituted, and -CH= in one or more rings may be replaced by -N=; ring express in One or more -CH2- in the ring may be replaced by -O-, and one or more single bonds in the ring may be replaced by double bonds; Ls1 and Ls3 each independently represent -F, -Cl, -CN, -NO2, -NCO, -NCS, -OCN, -SCN, -C(O)N(R S0 )2. -C(O)R S0 , a straight or branched alkyl group containing 1 to 12 carbon atoms, wherein one or more non-adjacent -CH2- in a straight-chain or branched alkyl group containing 1 to 12 carbon atoms can be independently replaced by -CH=CH-, -C≡C-, -O-, -CO-, -CO-O- or -O-CO-, and wherein a straight-chain or branched alkyl group containing 1 to 12 carbon atoms, One or more -H in the above-mentioned may be independently replaced by -F, wherein R S0 represents a straight or branched chain alkyl group containing 1 to 12 carbon atoms; Ls2 means R S2 and R S3 Each independently represents an anchoring group, the anchoring group is Where * indicates the connection site in the bonded structure; p represents 1 or 2, wherein when p represents 2, -Sp 8 -X 2 Can be the same or different; o means 0 or 1; M S1 express I S1 and J S1 Each independently represents -CH2-, -O- or -S-; N S1 Indicates =O or =S; V K1 、V K2 and V K3 Each independently represents -CH= or -N=; X 1 and X 2 Each independently represents -H, -OH, -SH, -NH2, -NHR 11 、-N(R 11 )2. -NHC(O)R 11 、-OR 11 , -C(O)OH, -CHO, or a linear or branched halogenated or unhalogenated alkyl group containing 1 to 12 carbon atoms, wherein X 1 and X 2 At least one of -OH, -SH, -NH2, -NHR 11 , -C(O)OH and -CHO, where R 11 represents a straight or branched chain alkyl group containing 1 to 12 carbon atoms; P1, P2, P3, P 1 , P 2 and P 3 each independently represents a polymerizable group; Sp1, Sp2, Sp3, Sp 1 、Sp 2 、Sp 3 、Sp 4 、Sp 5 、Sp 7 and Sp 8 each independently represents a spacer group or a single bond; Sp 6 Each independently expresses Z1, Z2, Z 1 and Z 2 Each independently represents -O-, -S-, -CO-, -CO-O-, -O-CO-, -O-CO-O-, -CH2O-, -OCH2-, -CH2S-, -SCH2-, -CF2O-, -OCF2-, -CF2S-, -SCF2-, -(CH2) d -, -CF2CH2-, -CH2CF2-, -(CF2) d -, -CH=CH-, -CF=CF-, -CH=CF-, -CF=CH-, -C≡C-, -CH=CH-CO-O-, -O-CO-CH=CH-, -CH2CH2-CO-O-, -O-CO-CH2CH2-, -CHR 1 -、-CR 1 R 2 - or a single bond, where R 1 and R 2 Each independently represents a straight or branched alkyl group containing 1 to 12 carbon atoms, and d represents an integer of 1 to 4; X B and X0 each independently represent -O-, -S- or -CO-; L B1 and L B2 Each independently represents -H, -F, -Cl, -CF3 or -OCF3; Z B1 and Z B2 Each independently represents a single bond, -O-, -S-, -CO-O-, -O-CO-, -CH2O-, -OCH2-, -CH=CH-, -C≡C-, -CH2CH2-, -CF2CF2-, -(CH2)4-, -CF2O- or -OCF2-; n B1 and n B2 Each independently represents 0, 1 or 2. B1 When it indicates 2, the ring can be the same or different, where n B2 When it indicates 2, the ring Can be the same or different, Z B2 Can be the same or different; n s1 Indicates 1, 2, or 3, n s2 represents 1, 2, 3, or 4, and n s1 +n s2 ≥3, where n s1 When it means 2 or 3, can be the same or different, where n s2 When it means 2, 3 or 4, Can be the same or different; p s1 、p s2 、p s3 and p s4 Each independently represents 0, 1 or 2, where p s1 When p represents 2, Ls2 can be the same or different. s2 When p represents 2, Ls1 can be the same or different. s3 When it means 2, -Sp 5 -RS 3 can be the same or different, where p s4 When it represents 2, Ls3 can be the same or different; a represents 0, 1 or 2, b represents 0 or 1, wherein when a represents 2, the ring can be the same or different, Z1 can be the same or different; R N1 and R N2 Each independently represents a straight or branched alkyl group containing 1 to 12 carbon atoms, One or more non-adjacent -CH2- in the linear or branched alkyl group containing 1 to 12 carbon atoms may be independently replaced by -CH=CH-, -C≡C-, -O-, -CO-, -CO-O- or -O-CO-; ring and ring Each independently expresses in One or more -CH2- in the ring may be replaced by -O-, and one or more single bonds in the ring may be replaced by double bonds, wherein One or more -H in the ring may be replaced by -F, -Cl or -CN, and one or more -CH= in the ring may be replaced by -N=; Z N1 and Z N2 Each independently represents a single bond, -CO-O-, -O-CO-, -CH2O-, -OCH2-, -C≡C-, -CH=CH-, -CH2CH2- or -(CH2)4-; L N1 and L N2 Each independently represents -H, an alkyl group containing 1 to 3 carbon atoms or a halogen; n N1 Represents 0, 1, 2, or 3, n N2 Represents 0 or 1, and 0≤n N1 +n N2 ≤3, when n N1 =2 or 3, the ring Can be the same or different, Z N1 Can be the same or different; When n N1 +n N2 = 1, and the rings are connected by single bonds, the rings or ring Not for When n N1 =2,n N2 =0, and Z N1 When all are single bonds, at least one ring Not for R M1 and R M2 Each independently represents a straight or branched alkyl group containing 1 to 12 carbon atoms, One or more non-adjacent -CH2- in the linear or branched alkyl group containing 1 to 12 carbon atoms may be independently replaced by -CH=CH-, -C≡C-, -O-, -CO-, -CO-O- or -O-CO-; ring ring and ring Each independently expresses in One or more -CH2- in the ring may be replaced by -O-, one or more single bonds in the ring may be replaced by double bonds, At most one -H in may be replaced by halogen; Z M1 and Z M2 Each independently represents a single bond, -CO-O-, -O-CO-, -CH2O-, -OCH2-, -C≡C-, -CH=CH-, -CH2CH2- or -(CH2)4-; n M represents 0, 1, or 2, where n M =2, ring Can be the same or different, Z M2 Can be the same or different; Wherein, the weight percentage of the compound of the general formula B in the liquid crystal composition is 0.1%-30%; the weight percentage of the compound of the general formula I in the liquid crystal composition is 0.1%-40%; the weight percentage of the polymerizable compound of the general formula RM in the liquid crystal composition is 0.001%-5%; the weight percentage of the compound of the general formula SA in the liquid crystal composition is 0.001%-5%; the weight percentage of the compound of the general formula M in the liquid crystal composition is 0.1%-60%; the weight percentage of the compound of the general formula N in the liquid crystal composition is 20%-40%; and The liquid crystal composition comprises at least one compound of the general formula I-1 and at least one compound of the general formula I-2.

2. The liquid crystal composition according to claim 1, characterized in that: The compound of formula B is selected from the group consisting of the following compounds: in, R B1 ' and R B2 ' Each independently represents a straight or branched alkyl group containing 1 to 12 carbon atoms.

3. The liquid crystal composition according to claim 1, characterized in that: The polymerizable compound of the general formula RM is selected from the group consisting of the following compounds: in, X1-X 10 , X 12 Each independently represents -F, -Cl, -Sp3-P3, a linear or branched alkyl or alkoxy group containing 1 to 5 carbon atoms, 4. The liquid crystal composition according to claim 1, characterized in that: The self-aligning agent of the general formula SA is selected from the group consisting of the following compounds: in, LS 31 Indicates -F, -Cl, -CN, -NO2, -NCO, -NCS, -OCN, -SCN, -C(O)N(R S0 )2. -C(O)R S0 , a straight or branched alkyl group containing 1 to 12 carbon atoms, wherein one or more non-adjacent -CH2- in a straight-chain or branched alkyl group containing 1 to 12 carbon atoms can be independently replaced by -CH=CH-, -C≡C-, -O-, -CO-, -CO-O- or -O-CO-, and wherein a straight-chain or branched alkyl group containing 1 to 12 carbon atoms, One or more -H in the above-mentioned may be independently replaced by -F, wherein R S0 represents a straight or branched chain alkyl group containing 1 to 12 carbon atoms; LS 21 Indicates -Sp 3 -P 2 or and Z 11 Represents -O-, -S-, -CO-, -CO-O-, -O-CO-, -O-CO-O-, -CH2O-, -OCH2-, -CH2S-, -SCH2-, -CF2O-, -OCF2-, -CF2S-, -SCF2-, -(CH2) d -, -CF2CH2-, -CH2CF2-, -(CF2) d -, -CH=CH-, -CF=CF-, -CH=CF-, -CF=CH-, -C≡C-, -CH=CH-CO-O-, -O-CO-CH=CH-, -CH2CH2-CO-O-, -O-CO-CH2CH2-, -CHR 1 -、-CR 1 R 2 - or a single bond, where R 1 and R 2 Each independently represents a linear or branched alkyl group containing 1 to 12 carbon atoms, and d represents an integer of 1-4.

5. The liquid crystal composition according to claim 1, characterized in that: The compound of the general formula N is selected from the group consisting of the following compounds:

6. The liquid crystal composition according to claim 1, characterized in that: The compound of formula M is selected from the group consisting of the following compounds:

7. A liquid crystal display device comprising the liquid crystal composition according to any one of claims 1 to 6.

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